Cardinal Health Presource Kits: 1) NEWNAN SMR PACK, Catalog Number: SEN21SPPMB
FDA Recall Z-2944-2026 · Posted 2026-08-13
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Recalling FirmCardinal Health 200, LLC
Recall StatusOpen, Classified
Product CodeOEZ
Date Initiated2026-07-14
Product Quantity80 kits
Reason for Recall
Cardinal Health was recently informed of a medical device recall from MEDICOM concerning the Ritmed Neurological Sponges. The recall is being issued due to unexpected variability of endotoxin levels on the products.
Firm Action
Cardinal Health issued an URGENT: PRODUCT CORRECTION notice to its consignees on 7/14/2026 via FedEx. The notice explained the issue and enclosed a copy of the recall notice issued by the supplier of the affected component which explained the risk and provided details on the affected component.
The notice issued by Cardinal Health requested that consignee notify its clinicians, affix a warning label to the affected kits in their inventory, and respond using the acknowledgement form via fax to 614.652.9648. Additional labels will be sent to your facility upon request. Please send an email to:
[email protected]. The warning label requests that the affected component be removed and discarded.
For component credit or replacement, please contact the following:
" Hospitals Cardinal Customer Service at 866.551.0533
" Distributors Distributor Management at 800.635.6021
" Federal Government facilities Government Customer Service at 800.444.1166.
Distributors were direct to notify their customers.
For questions, additional labels, or desire special assistance relating to this
recall, please feel free to contact Cardinal Health Quality Systems at 800.292.9332.
Root Cause
Nonconforming Material/Component
Distribution Pattern
US Nationwide. Canada.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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